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HRID 2426001作成日:2026年10月25日

Diisopropylethylamine → 1-(2-(3,5-Dimethoxybenzylamino)-4-fluorophenyl)-2,2,2-trifluoroethanone

https://huagongshe.com/reaction/2426001

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物(3,5-Dimethoxyphenyl)methanamineHCID 420973—
反応物1-(2,4-Difluorophenyl)-2,2,2-trifluoroethanoneHCID 24726837—
溶媒AcetonitrileHCID 6342—
生成物1-(2-(3,5-Dimethoxybenzylamino)-4-fluorophenyl)-2,2,2-trifluoroethanoneHCID 58707272100.9%

反応手順

A solution of (3,5-dimethoxyphenyl)methanamine (0.88 g, 5.20 mmol), 2,2,2-trifluoro-1-(2,4-difluorophenyl)ethanone (1.0 g, 4.80 mmol) and diisopropylethylamine (1.6 mL, 9.6 mmol) in acetonitrile was stirred at 40° C. for 48 h. The solvent was concentrated in vacuo, the residue was taken up in dichloromethane and washed with water and brine, dried, and concentrated under reduced pressure to yield 1.73 g of a yellow oil. The residue was purified by PTLC (20% ethyl acetate in hexanes) to give 527 mg (35%) of the desired aniline: 1H NMR (400 MHz, CDCl3) δ 9.27 (br t, 1H), 7.83 (br s, 1H), 6.47-6.40 (m, 5H), 4.42 (d, 2H), 3.79 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07968538B2
出典データセットuspto-grants-2011_06
ORD IDord-64fc5c17107a4f758c4f2f1b3ef7bc58
出典メモuspto-grants-2011_06